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Sildenafil Citrate

NDC 52817-295, Sildenafil, tablet, film coated, from TruPharma LLC.

Product NDC
52817-295
Status
Listed
Labeler
TruPharma LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204883
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/52817-295 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SILDENAFIL CITRATE20 mg/1

Pharmacologic classes

Phosphodiesterase 5 Inhibitor [EPC]; Phosphodiesterase 5 Inhibitors [MoA]

Package NDCNDC-11Package
52817-295-00528170295001000 TABLET, FILM COATED in 1 BOTTLE (52817-295-00)
52817-295-905281702959090 TABLET, FILM COATED in 1 BOTTLE (52817-295-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c8864c64-22ad-402b-a1e8-cfb53fa02e80

  • NADAC price for package 52817029590

    GET /v1/drugs/nadac/52817029590

Use it

Look up 52817-295 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/52817-295 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 52817-295. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.